Harp Bhakti Petigara, Belai Nebebech, Barrows Julie N
U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition, Office of Cosmetics and Colors, 5100 Paint Branch Pkwy, College Park, MD 20740, USA.
J AOAC Int. 2011 Sep-Oct;94(5):1548-54. doi: 10.5740/jaoacint.10-474.
An ultra-performance liquid chromatography (UPLC) method was developed to determine the manufacturing intermediates and subsidiary colors in the monosulfo monoazo color additive D&C Red No. 34 and its lakes. This method is currently used for batch certification of the color additives by the U.S. Food and Drug Administration to ensure that each lot meets published specifications for coloring drugs and cosmetics. The new UPLC method has replaced an HPLC method for determining the intermediates and a TLC method for determining the subsidiary colors. The intermediates are 2-amino-1-naphthalenesulfonic acid (Tobias acid) and 3-hydroxy-2-naphthalenecarboxylic acid (3-hydroxy-2-naphthoic acid). Subsidiary colors are positional isomers of the major dye component or related compounds containing lower numbers of substituent groups. The analytes are identified by comparison of their UPLC retention times and UV or visible absorption spectra with those of standards. Validation studies showed that peak area calibrations for the analytes were generally linear (R > 0.999), and recoveries were 98-103%. The LODs were 0.002-0.02%, and the RSDs at the specification levels were 0.7-2.2%. Survey analyses of 12 samples of certified D&C Red No. 34 straight colors and lakes from six domestic and foreign manufacturers yielded results for the intermediates by UPLC and HPLC that were consistent within experimental error. The UPLC analyses yielded results for the subsidiary colors that were consistently lower than results previously obtained by TLC, which we attribute to limitations of the TLC method. The new UPLC method provides sharper peaks, better peak separation, and faster analysis times than the formerly used HPLC method and is more accurate, much faster, and much less labor-intensive than the formerly used TLC method.
开发了一种超高效液相色谱(UPLC)方法,用于测定单磺酸单偶氮食用色素D&C红34号及其色淀中的生产中间体和副色。该方法目前被美国食品药品监督管理局用于食用色素的批次认证,以确保每一批次都符合药品和化妆品着色的公布规格。新的UPLC方法取代了用于测定中间体的HPLC方法和用于测定副色的TLC方法。中间体为2-氨基-1-萘磺酸(托拜厄斯酸)和3-羟基-2-萘甲酸(3-羟基-2-萘酸)。副色是主要染料成分的位置异构体或含较少取代基的相关化合物。通过将分析物的UPLC保留时间和紫外或可见吸收光谱与标准品进行比较来鉴定分析物。验证研究表明,分析物的峰面积校准通常呈线性(R>0.999),回收率为98-103%。检测限为0.002-0.02%,规格水平下的相对标准偏差为0.7-2.2%。对来自国内外六家制造商的12个经认证的D&C红34号纯色和色淀样品进行的调查分析,通过UPLC和HPLC得到的中间体结果在实验误差范围内一致。UPLC分析得到的副色结果始终低于之前通过TLC获得的结果,我们将其归因于TLC方法的局限性。与之前使用的HPLC方法相比,新的UPLC方法提供了更尖锐的峰、更好的峰分离和更快的分析时间,并且比之前使用的TLC方法更准确、更快且劳动强度更低。